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Medical Device

T1 Patient Monitor. Operator's Manual: T1 Patient Monitor

Recall date: 2026-10-14 · Source: FDA_DEVICE
Brand / Firm
Mindray DS USA, Inc.
Product
T1 Patient Monitor. Operator's Manual: T1 Patient Monitor
Reason for recall
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Units affected
4,946 units
Description
T1 Patient Monitor. Operator's Manual: T1 Patient Monitor
View official recall notice →